A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6123619



Internal ID9072252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182522206..182522811hg38UCSC Ensembl
chr3:182239994..182240599hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38606
hg19606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659235
Supporting Variants
SamplesHG01047
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6123619
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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